Use your antibodies-online credentials, if available.
Il n’y a pas de produits dans votre liste de comparaison.
Votre panier est vide.
The protein encoded by MID1 is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins.
Showing 10 out of 66 products:
Human Polyclonal MID1 Primary Antibody pour WB - ABIN439762
Bell, Malyukova, Holien, Koach, Parker, Kavallaris, Marshall, Cheung: TRIM16 acts as an E3 ubiquitin ligase and can heterodimerize with other TRIM family members. dans PLoS ONE 2012
Human Monoclonal MID1 Primary Antibody pour ELISA, WB - ABIN517934
Liu, Knutzen, Krauss, Schweiger, Chiang: Control of mTORC1 signaling by the Opitz syndrome protein MID1. dans Proceedings of the National Academy of Sciences of the United States of America 2011
Data show that protein phosphatase-2A (PP2A (Montrer PPP2R4 Anticorps)) was upregulated in lung adenocarcinoma cell lines that were transfected with midline 1 E3 ubiquitin-protein ligase (Montrer UBE2K Anticorps) (MID1)-siRNA, suggesting MID1 negatively regulates PP2A (Montrer PPP2R4 Anticorps) in lung adenocarcinoma.
identified four miRNAs, miR (Montrer MLXIP Anticorps)-19, miR (Montrer MLXIP Anticorps)-340, miR (Montrer MLXIP Anticorps)-374 and miR (Montrer MLXIP Anticorps)-542 that bind to the 3'-UTR (Montrer UTS2R Anticorps) of the MID1 mRNA. These miRNAs not only regulate MID1 expression but also mTOR (Montrer FRAP1 Anticorps) signaling and translation of disease associated mRNAs and could therefore serve as potential drugs for future therapy development
Our data reveal a novel role for MID1 and for atypical ubiquitination in balancing BRAF35 (Montrer HMG20B Anticorps) presence, and likely its activity, within nuclear and cytoplasmic compartments
P151L MID1 mutation is associated with X-linked Opitz Syndrome.
the coiled-coil and COS domain (CC-COS) bind to microtubules, demonstrating for the first time that MID1 can directly associate with the microtubules
Osx is upregulated in patients with Ossification of the posterior longitudinal ligament.
A130T/V mutations within the MID1 zinc-binding Bbox1 (Montrer BBOX1 Anticorps) domain affects protein folding.
MID1 catalyzes the ubiquitination of protein phosphatase 2A and mutations within its Bbox1 (Montrer BBOX1 Anticorps) domain disrupt polyubiquitination of alpha4 but not of PP2Ac (Montrer PPP2CA Anticorps) in X-linked Opitz syndrome.
TRAIL regulates MID1 and TSLP (Montrer TSLP Anticorps), inflammation, fibrosis, smooth muscle hypertrophy, and expression of inflammatory effector chemokines and cytokines in experimental eosinophilic esophagitis.
These studies provide insight into the mechanism by which mutations observed in X-linked Opitz G syndrome affect the structure and function of the MID1 Bbox1 (Montrer BBOX1 Anticorps) domain
we show that MID1 controls exocytosis of lytic granules and cytotoxicity in murine cytotoxic lymphocytes
X-linked microtubule-associated protein (Montrer SPAG5 Anticorps), Mid1, regulates axon development.
MID1 inhibition also limited rhinovirus-induced exacerbation of allergic airway disease
Thus, lack of Mid1 causes a misspecification of the midbrain/cerebellar boundary that results in an abnormal development of the most anterior cerebellar lobes.
Analysis of Mid1, Hccs (Montrer HCCS Anticorps), Arhgap6 (Montrer ARHGAP6 Anticorps), and Msl3l1 (Montrer MSL3 Anticorps) in X-linked polydactyly (Xpl) and Patchy-fur (Paf (Montrer PAF Anticorps)) mutant mice
SHH (Montrer SHH Anticorps)-dependent E-ligase Midline1 regulates ubiquitin-mediated proteasomal degradation of Pax6 (Montrer PAX6 Anticorps) during visual system development.
The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Multiple different transcript variants are generated by alternate splicing\; however, the full-length nature of some of the variants has not been determined.
RING finger protein 59
, midline 1 RING finger protein
, putative transcription factor XPRF
, tripartite motif protein TRIM18
, tripartite motif-containing protein 18
, zinc finger on X and Y, mouse, homolog of
, Finger on X and Y (in rat only on X)
, E3 ubiquitin-protein ligase Midline-1
, midline 1 (Opitz/BBB syndrome)